Catalog Number

ASA-25090-S

Brand Name

ARROW

Version/Model Number

IPN040082

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

Yes

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

BSP

Product Code Name

NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

Public Device Record Key

3a718f34-4067-49dd-a169-ee322c589aea

Public Version Date

November 05, 2018

Public Version Number

3

DI Record Publish Date

September 16, 2016

Package DI Number

30801902074240

Quantity per Package

5

Contains DI Package

00801902074249

Package Discontinue Date

October 30, 2018

Package Status

Not in Commercial Distribution

Package Type

Box